HCSGD entry for CDCA2


1. General information

Official gene symbolCDCA2
Entrez ID157313
Gene full namecell division cycle associated 2
Other gene symbolsRepo-Man
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005634NucleusIDAcellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0007067MitosisIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.86312121120.00013876750.99999024730.0206355932

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Down-0.4123404146
GSE13712_SHEARDown-0.6332659440
GSE13712_STATICUp0.1028923016
GSE19018Up0.2010889733
GSE19899_A1Down-0.7334095995
GSE19899_A2Down-3.7255728852
PubMed_21979375_A1Down-1.4572340581
PubMed_21979375_A2Down-2.4681659527
GSE35957Down-1.2956004769
GSE36640Down-4.9008564898
GSE54402Down-1.1179331064
GSE9593Down-0.3306877126
GSE43922Down-1.3411020170
GSE24585Down-0.1105231954
GSE37065Down-0.4156760930
GSE28863_A1Up0.3137846719
GSE28863_A2Up1.3145661978
GSE28863_A3Down-0.5302735407
GSE28863_A4Down-0.0410680493
GSE48662Down-2.1174432646

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-193b-3pMIMAT0002819MIRT016459MicroarrayFunctional MTI (Weak)20304954
hsa-miR-18a-3pMIMAT0002891MIRT040857CLASHFunctional MTI (Weak)23622248
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  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

24905922Results allowed us to identify Cell Division Cycle Associated 2 (CDCA2) and Inhibitor of DNA binding/differentiation type 4 (ID4) as novel targets of SAmiR-494 and SAmiR-486-5p, respectively
24905922Furthermore, we demonstrated that the over-expression of CDCA2 in human primary fibroblasts was able to partially counteract etoposide-induced senescence by mitigating the activation of DNA Damage Response
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